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采用超高效液相色谱-串联质谱法对血清叶酸维生素异构体进行多重检测。

Multiplex Measurement of Serum Folate Vitamers by UPLC-MS/MS.

作者信息

Meadows Sarah

机构信息

MRC Human Nutrition Research, Cambridge, CB1 9NL, UK.

出版信息

Methods Mol Biol. 2017;1546:245-256. doi: 10.1007/978-1-4939-6730-8_21.

Abstract

The implementation of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to measure six folate vitamers in serum samples allows a more individual and accurate measurement than the commonly used immunoassays. In the described method, serum samples undergo solid phase extraction followed by liquid chromatography coupled with electrospray ionization tandem mass spectrometry with a run time of 3.5 min. Recovery is 95 % for the most important folate metabolite, 5-methyltetrahydrofolate (MTHF), and greater than 78 % for other minor folate forms. The limit of detection ranges from 0.2 to 0.4 nmol/L with a intra-batch imprecision of less than 7 % for all analytes and calibration ranges of 1-100 nmol/L for MTHF and 0.5-20 nmol/L for the minor folate forms, with greater than 0.99 R linearity.

摘要

液相色谱-串联质谱法(LC-MS/MS)用于测量血清样本中的六种叶酸维生素异构体,与常用的免疫测定法相比,它能实现更个性化、更准确的测量。在所描述的方法中,血清样本先进行固相萃取,然后进行液相色谱联用电喷雾电离串联质谱分析,运行时间为3.5分钟。对于最重要的叶酸代谢物5-甲基四氢叶酸(MTHF),回收率为95%,对于其他次要叶酸形式,回收率大于78%。检测限范围为0.2至0.4 nmol/L,所有分析物的批内不精密度小于7%,MTHF的校准范围为1-100 nmol/L,次要叶酸形式的校准范围为0.5-20 nmol/L,线性大于0.99R。

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